Sequential oxidation procedures with KMnO4: Component characteristics of labile reducing capacity fractions in anaerobic sediments.

IF 8.2 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Science of the Total Environment Pub Date : 2024-12-10 Epub Date: 2024-10-30 DOI:10.1016/j.scitotenv.2024.177126
Xuemei Chen, Zhijun Li, Songjie Fu, Lanwei Liang, Xiaohan Liu, Fang Hu, Wen Zhang, Yonghong Bi, Yang Jiao, Sen Gu, Qingman Li
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引用次数: 0

Abstract

Reducing substances are a mixture of different forms and types and play extremely important roles in manipulating the redox status of sediments, benthic habitats, and substance exchanges at the sediment-water interface in aquatic ecosystems. However, little is known about their abundance, forms, and reducibility in sediments. In this study, the procedures were developed to sequentially fractionate sediment reducing capacity (RC) fractions with the pH dependence of KMnO4 oxidability. The procedures were then applied to 60 sediments from 2 lakes and 3 reservoirs, generating an RCpH7.0 fraction (oxidized at ~0.48 V [reference: SHE]) and an RCpH2.0 fraction (oxidized at ~0.95 V [reference: SHE]), and the component of each fraction was characterized. The RCpH7.0 fraction amounted to 45.4 ± 25.9 cmol e-·kg-1 DW, and the RCpH2.0 fraction amounted to 42.8 ± 22.9 cmol e-·kg-1 DW; fraction sizes depended greatly on sediment origin. Reducing organic substances (ROS) were the main contributors to the RC fractions, with mean value of 30.0 ± 24.1 and 38.5 ± 22.2 cmol e-·kg-1 DW in RCpH7.0 (% contribution: 68.0 ± 5.3 % of RCpH7.0) and RCpH2.0 (90.0 ± 1.5 % of RCpH2.0), respectively. The next contributor was Fe(II), with mean value of 13.5 ± 8.2 and 3.8 ± 3.7 cmol e-·kg-1 DW in RCpH7.0 (28.3 ± 5.2 %) and in RCpH2.0 (9.9 ± 8.6 %), respectively. The smallest component was sulfide (Sn), which had a mean of 2.0 ± 3.1 cmol e-·kg-1 DW in RCpH7.0 and was essentially negligible in RCpH2.0. The number of electrons lost per mole of reducing substances (Ni) differed between the two RC fractions and among sediments of different origins. NROS was lower in the RCpH7.0 fraction (0.22 ± 0.09) compared to the RCpH2.0 fraction (0.31 ± 0.12) and significantly related to levels of active Fe(III) and sulfides (Sn) (p < 0.05). The opposite pattern was seen for NFe(II) and NSn. Based on the compositive reducing capacity (CRC) for the RCpH7.0 fraction, sediment redox status could be classified as ROS-Fe(II) (3.8 ± 1.7 cmol e-·kg-1 DW) or ROS-Sn (10.1 ± 4.8 cmol e-·kg-1 DW) (weaker vs. stronger, respectively; p < 0.01). The RC-based index provides a more comprehensive perspective on characterizing sediment redox status compared to the Eh.

使用 KMnO4 的顺序氧化程序:厌氧沉积物中易变还原能力组分的特征。
还原性物质是不同形式和类型的混合物,在操纵沉积物、底栖栖息地的氧化还原状态以及水生生态系统中沉积物-水界面的物质交换方面发挥着极其重要的作用。然而,人们对它们在沉积物中的丰度、形式和还原性知之甚少。在本研究中,我们开发了一套程序,用于根据 KMnO4 氧化性的 pH 值依次分馏沉积物还原能力(RC)组分。然后将这些程序应用于来自 2 个湖泊和 3 个水库的 60 个沉积物,产生了一个 RCpH7.0 组分(在 ~0.48 V [参考值:SHE] 下氧化)和一个 RCpH2.0 组分(在 ~0.95 V [参考值:SHE] 下氧化),并对每个组分的成分进行了表征。RCpH7.0 部分为 45.4 ± 25.9 cmol e--kg-1 DW,RCpH2.0 部分为 42.8 ± 22.9 cmol e--kg-1 DW;各部分的大小在很大程度上取决于沉积物的来源。还原性有机物(ROS)是 RC 产物的主要贡献者,在 RCpH7.0 和 RCpH2.0 中的平均值分别为 30.0 ± 24.1 和 38.5 ± 22.2 cmol e--kg-1 DW(贡献率:RCpH7.0 的 68.0 ± 5.3 %)和 RCpH2.0 的 90.0 ± 1.5 %。其次是铁(II),RCpH7.0(28.3 ± 5.2 %)和 RCpH2.0(9.9 ± 8.6 %)中的平均值分别为 13.5 ± 8.2 和 3.8 ± 3.7 cmol e--kg-1 DW。最小的成分是硫化物(Sn),在 RCpH7.0 中的平均值为 2.0 ± 3.1 cmol e--kg-1 DW,而在 RCpH2.0 中基本上可以忽略不计。每摩尔还原性物质(镍)损失的电子数在两种 RC 分馏物之间以及不同来源的沉积物之间存在差异。与 RCpH2.0 组分(0.31 ± 0.12)相比,RCpH7.0 组分(0.22 ± 0.09)的 NROS 较低,并且与活性铁(III)和硫化物(Sn)(p 铁(II)和 NSn)的含量显著相关。根据 RCpH7.0 分馏物的合成还原能力 (CRC),沉积物的氧化还原状态可分为 ROS-Fe(II)(3.8 ± 1.7 cmol e--kg-1 DW)或 ROS-Sn(10.1 ± 4.8 cmol e--kg-1 DW)(分别为较弱与较强; p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science of the Total Environment
Science of the Total Environment 环境科学-环境科学
CiteScore
17.60
自引率
10.20%
发文量
8726
审稿时长
2.4 months
期刊介绍: The Science of the Total Environment is an international journal dedicated to scientific research on the environment and its interaction with humanity. It covers a wide range of disciplines and seeks to publish innovative, hypothesis-driven, and impactful research that explores the entire environment, including the atmosphere, lithosphere, hydrosphere, biosphere, and anthroposphere. The journal's updated Aims & Scope emphasizes the importance of interdisciplinary environmental research with broad impact. Priority is given to studies that advance fundamental understanding and explore the interconnectedness of multiple environmental spheres. Field studies are preferred, while laboratory experiments must demonstrate significant methodological advancements or mechanistic insights with direct relevance to the environment.
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